2015년 2월 25일 수요일

Nature Genetics Contents: March 2015 pp 187 - 304


Nature Genetics

TABLE OF CONTENTS

March 2015 Volume 47, Issue 3
Editorial
Correspondence
News and Views
Research Highlights
Analysis
Articles
Letters
Technical Reports
Corrigenda
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EDITORIAL


Announcement: double-blind peer review   p187
doi:10.1038/ng.3238
Nature and its sister journals start offering anonymity to authors during the peer-review process.

CORRESPONDENCE


Evolution of Tibetan wild boars   pp188 - 189
Laurent A F Frantz, Ole Madsen, Hendrik-Jan Megens, Joshua G Schraiber, Yogesh Paudel, Mirte Bosse, Richard P M A Crooijmans, Greger Larson & Martien A M Groenen
doi:10.1038/ng.3197
Reply to 'Evolution of Tibetan wild boars'   pp189 - 190
Mingzhou Li, Ying Li, Carol K L Yeung, Shilin Tian, Xuewei Li & Ruiqiang Li
doi:10.1038/ng.3194
On genetic differentiation between domestic pigs and Tibetan wild boars   pp190 - 192
Miguel Pérez-Enciso, William Burgos-Paz & Sebastián E Ramos-Onsins
doi:10.1038/ng.3191
Reply to 'On genetic differentiation between domestic pigs and Tibetan wild boars'   p192
Mingzhou Li, Carol K L Yeung, Ying Li, Shilin Tian, Xuewei Li & Ruiqiang Li
doi:10.1038/ng.3193

NEWS AND VIEWS



YAP and the drug resistance highway   pp193 - 194
Alona Keren-Paz, Rafi Emmanuel & Yardena Samuels
doi:10.1038/ng.3228
Deciphering mechanisms of drug resistance is crucial to winning the battle against cancer. A new study points to an unexpected function of YAP in drug resistance and illuminates its potential role as a therapeutic target.

See also: Letter by Lin et al.
Avalanching mutations in biallelic mismatch repair deficiency syndrome   pp194 - 196
Joshua J Waterfall & Paul S Meltzer
doi:10.1038/ng.3227
Tumors from pediatric patients generally contain relatively few somatic mutations. A new study reports a striking exception in individuals in whom biallelic germline deficiency for mismatch repair is compounded by somatic loss of function in DNA proofreading polymerases, resulting in 'ultra-hypermutated' malignant brain tumors.

See also: Letter by Shlien et al.
Big Bang and context-driven collapse   pp196 - 197
Mark Robertson-Tessi & Alexander R A Anderson
doi:10.1038/ng.3231
Heterogeneity is the single most important factor driving cancer progression and treatment failure, yet little is understood about how and when this heterogeneity arises. A new study shows that colorectal cancers acquire their dominant mutations early in development and that subsequent mutations, even if they confer greater fitness, are unlikely to sweep through the tumor.

See also: Article by Sottoriva et al.

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RESEARCH HIGHLIGHTS


Enhancer evolution in mammals | Long-term memory genes in C. elegans | Rb links reprogramming and cancer | Micropeptide regulates muscle performance | Stem cell metabolic and epigenetic reprogramming

ANALYSIS


The landscape of long noncoding RNAs in the human transcriptome   pp199 - 208
Matthew K Iyer, Yashar S Niknafs, Rohit Malik, Udit Singhal, Anirban Sahu, Yasuyuki Hosono, Terrence R Barrette, John R Prensner, Joseph R Evans, Shuang Zhao, Anton Poliakov, Xuhong Cao, Saravana M Dhanasekaran, Yi-Mi Wu, Dan R Robinson, David G Beer, Felix Y Feng, Hariharan K Iyer & Arul M Chinnaiyan
doi:10.1038/ng.3192
Arul Chinnaiyan and colleagues report the curation of 7,256 RNA sequencing libraries from tumors, normal tissues and cell lines. They find 58,648 lncRNAs, of which 79% are previously unnannotated.

ARTICLES


A Big Bang model of human colorectal tumor growth   pp209 - 216
Andrea Sottoriva, Haeyoun Kang, Zhicheng Ma, Trevor A Graham, Matthew P Salomon, Junsong Zhao, Paul Marjoram, Kimberly Siegmund, Michael F Press, Darryl Shibata & Christina Curtis
doi:10.1038/ng.3214
Christina Curtis, Darryl Shibata and colleagues report genomic profiling of 349 individual glands sampled from 15 human colorectal tumors. They observe high within-tumor heterogeneity and mixing of subclones in distant tumor regions, supporting a model whereby tumor growth occurs predominantly as a single expansion, with most detectable subclonal mutations arising during the earliest phases of tumor growth.

See also: News and Views by Robertson-Tessi & Anderson
Adaptation and possible ancient interspecies introgression in pigs identified by whole-genome sequencing   pp217 - 225
Huashui Ai, Xiaodong Fang, Bin Yang, Zhiyong Huang, Hao Chen, Likai Mao, Feng Zhang, Lu Zhang, Leilei Cui, Weiming He, Jie Yang, Xiaoming Yao, Lisheng Zhou, Lijuan Han, Jing Li, Silong Sun, Xianhua Xie, Boxian Lai, Ying Su, Yao Lu, Hui Yang, Tao Huang, Wenjiang Deng, Rasmus Nielsen, Jun Ren & Lusheng Huang
doi:10.1038/ng.3199
Lusheng Huang, Jun Ren and colleagues report the genome sequences of 69 pigs, representing 11 geographically distinct breeds and 3 wild boar populations, from within China. They identify loci related to high- and low-latitude adaptation and infer a likely ancient introgression event in northern Chinese pigs.
Genetic architecture of artemisinin-resistantPlasmodium falciparum   pp226 - 234
Olivo Miotto, Roberto Amato, Elizabeth A Ashley, Bronwyn MacInnis, Jacob Almagro-Garcia, Chanaki Amaratunga, Pharath Lim, Daniel Mead, Samuel O Oyola, Mehul Dhorda, Mallika Imwong, Charles Woodrow, Magnus Manske, Jim Stalker, Eleanor Drury, Susana Campino, Lucas Amenga-Etego, Thuy-Nhien Nguyen Thanh, Hien Tinh Tran, Pascal Ringwald, Delia Bethell, Francois Nosten, Aung Pyae Phyo, Sasithon Pukrittayakamee, Kesinee Chotivanich, Char Meng Chuor, Chea Nguon, Seila Suon, Sokunthea Sreng, Paul N Newton, Mayfong Mayxay, Maniphone Khanthavong, Bouasy Hongvanthong, Ye Htut, Kay Thwe Han, Myat Phone Kyaw, Md Abul Faiz, Caterina I Fanello, Marie Onyamboko, Olugbenga A Mokuolu, Christopher G Jacob, Shannon Takala-Harrison, Christopher V Plowe, Nicholas P Day, Arjen M Dondorp, Chris C A Spencer, Gilean McVean, Rick M Fairhurst, Nicholas J White & Dominic P Kwiatkowski
doi:10.1038/ng.3189
Dominic Kwiatkowski and colleagues report a large multicenter genome-wide association study of Plasmodium falciparum resistance to artemisinin. They identify markers of a genetic background on which kelch13 mutations conferring artemisinin resistance are likely to emerge.
The genomic and phenotypic diversity ofSchizosaccharomyces pombe   pp235 - 241
Daniel C Jeffares, Charalampos Rallis, Adrien Rieux, Doug Speed, Martin Převorovský, Tobias Mourier, Francesc X Marsellach, Zamin Iqbal, Winston Lau, Tammy M K Cheng, Rodrigo Pracana, Michael Mülleder, Jonathan L D Lawson, Anatole Chessel, Sendu Bala, Garrett Hellenthal, Brendan O'Fallon, Thomas Keane, Jared T Simpson, Leanne Bischof, Bartlomiej Tomiczek, Danny A Bitton, Theodora Sideri, Sandra Codlin, Josephine E E U Hellberg, Laurent van Trigt, Linda Jeffery, Juan-Juan Li, Sophie Atkinson, Malte Thodberg, Melanie Febrer, Kirsten McLay, Nizar Drou, William Brown, Jacqueline Hayles, Rafael E Carazo Salas, Markus Ralser, Nikolas Maniatis, David J Balding, Francois Balloux, Richard Durbin & Jürg Bähler
doi:10.1038/ng.3215
Daniel Jeffares, Jurg Bahler and colleagues report the genome sequences of 161 natural isolates of Schizosaccharomyces pombe, finding moderate genetic diversity and weak global population structure. They also report genome-wide association studies for 223 quantitative traits.
Evolutionary history and global spread of theMycobacterium tuberculosis Beijing lineage   pp242 - 249
Matthias Merker, Camille Blin, Stefano Mona, Nicolas Duforet-Frebourg, Sophie Lecher, Eve Willery, Michael G B Blum, Sabine Rüsch-Gerdes, Igor Mokrousov, Eman Aleksic, Caroline Allix-Béguec, Annick Antierens, Ewa Augustynowicz-Kopeć, Marie Ballif, Francesca Barletta, Hans Peter Beck, Clifton E Barry III, Maryline Bonnet, Emanuele Borroni, Isolina Campos-Herrero, Daniela Cirillo, Helen Cox, Suzanne Crowe, Valeriu Crudu, Roland Diel, Francis Drobniewski, Maryse Fauville-Dufaux, Sébastien Gagneux, Solomon Ghebremichael, Madeleine Hanekom, Sven Hoffner, Wei-wei Jiao, Stobdan Kalon, Thomas A Kohl, Irina Kontsevaya, Troels Lillebæk, Shinji Maeda, Vladyslav Nikolayevskyy, Michael Rasmussen, Nalin Rastogi, Sofia Samper, Elisabeth Sanchez-Padilla, Branislava Savic, Isdore Chola Shamputa, Adong Shen, Li-Hwei Sng, Petras Stakenas, Kadri Toit, Francis Varaine, Dragana Vukovic, Céline Wahl, Robin Warren, Philip Supply, Stefan Niemann & Thierry Wirth
doi:10.1038/ng.3195
Thierry Wirth, Philip Supply, Stefan Niemann and colleagues analyze 4,987 Mycobacterium tuberculosis strains of the Beijing lineage isolated from 99 countries. They report whole-genome sequencing of 110 representative strains, characterize global population structure and reconstruct the evolutionary history of this lineage.

LETTERS


The Hippo effector YAP promotes resistance to RAF- and MEK-targeted cancer therapies   pp250 - 256
Luping Lin, Amit J Sabnis, Elton Chan, Victor Olivas, Lindsay Cade, Evangelos Pazarentzos, Saurabh Asthana, Dana Neel, Jenny Jiacheng Yan, Xinyuan Lu, Luu Pham, Mingxue M Wang, Niki Karachaliou, Maria Gonzalez Cao, Jose Luis Manzano, Jose Luis Ramirez, Jose Miguel Sanchez Torres, Fiamma Buttitta, Charles M Rudin, Eric A Collisson, Alain Algazi, Eric Robinson, Iman Osman, Eva Muñoz-Couselo, Javier Cortes, Dennie T Frederick, Zachary A Cooper, Martin McMahon, Antonio Marchetti, Rafael Rosell, Keith T Flaherty, Jennifer A Wargo & Trever G Bivona
doi:10.1038/ng.3218
Trever Bivona and colleagues show that the Hippo pathway effector YAP promotes resistance to RAF and MEK inhibitor therapy in multiple types of BRAF-mutant tumors. The findings suggest that combined suppression of YAP and RAF-MEK signaling might enhance treatment response and prevent drug resistance.

See also: News and Views by Keren-Paz et al.
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers   pp257 - 262
Adam Shlien, Brittany B Campbell, Richard de Borja, Ludmil B Alexandrov, Daniele Merico, David Wedge, Peter Van Loo, Patrick S Tarpey, Paul Coupland, Sam Behjati, Aaron Pollett, Tatiana Lipman, Abolfazl Heidari, Shriya Deshmukh, Na'ama Avitzur, Bettina Meier, Moritz Gerstung, Ye Hong, Diana M Merino, Manasa Ramakrishna, Marc Remke, Roland Arnold, Gagan B Panigrahi, Neha P Thakkar, Karl P Hodel, Erin E Henninger, A Yasemin Göksenin, Doua Bakry, George S Charames, Harriet Druker, Jordan Lerner-Ellis, Matthew Mistry, Rina Dvir, Ronald Grant, Ronit Elhasid, Roula Farah, Glenn P Taylor, Paul C Nathan, Sarah Alexander, Shay Ben-Shachar, Simon C Ling, Steven Gallinger, Shlomi Constantini, Peter Dirks, Annie Huang, Stephen W Scherer, Richard G Grundy, Carol Durno, Melyssa Aronson, Anton Gartner, M Stephen Meyn, Michael D Taylor, Zachary F Pursell, Christopher E Pearson, David Malkin, P Andrew Futreal, Michael R Stratton, Eric Bouffet, Cynthia Hawkins, Peter J Campbell, Uri Tabori & for the Biallelic Mismatch Repair Deficiency Consortium
doi:10.1038/ng.3202
Adam Shlien, Peter Campbell, Uri Tabori and colleagues report genome and exome sequencing of biallelic mismatch repair deficiency cancer samples from 12 children, including 10 high-grade gliomas. The hypermutational signature of the malignant glioma samples was consistent with a driver role for observed mutations in DNA polymerases ε or δ.

See also: News and Views by Waterfall & Meltzer
Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss   pp263 - 266
Heng Xu, Giles W Robinson, Jie Huang, Joshua Yew-Suang Lim, Hui Zhang, Johnnie K Bass, Alberto Broniscer, Murali Chintagumpala, Ute Bartels, Sri Gururangan, Tim Hassall, Michael Fisher, Richard Cohn, Tetsuji Yamashita, Tal Teitz, Jian Zuo, Arzu Onar-Thomas, Amar Gajjar, Clinton F Stewart & Jun J Yang
doi:10.1038/ng.3217
Jun Yang, Clinton Stewart and colleagues report the results of a genome-wide association study of cisplatin-induced ototoxicity among children undergoing treatment for brain tumors. They identify common variants in ACYP2 strongly associated with cisplatin-induced hearing loss and ototoxicity severity.
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy   pp267 - 271
Hong Liu, Astrid Irwanto, Xi'an Fu, Gongqi Yu, Yongxiang Yu, Yonghu Sun, Chuan Wang, Zhenzhen Wang, Yukinori Okada, Huiqi Low, Yi Li, Herty Liany, Mingfei Chen, Fangfang Bao, Jinghui Li, Jiabao You, Qilin Zhang, Jian Liu, Tongsheng Chu, Anand Kumar Andiappan, Na Wang, Guiye Niu, Dianchang Liu, Xiulu Yu, Lin Zhang, Hongqing Tian, Guizhi Zhou, Olaf Rotzschke, Shumin Chen, Xuejun Zhang, Jianjun Liu & Furen Zhang
doi:10.1038/ng.3212
Furen Zhang and colleagues report the results of a three-stage genome-wide association study of leprosy in the Chinese population. They discover six new susceptibility loci and observe substantial overlap with loci previously implicated in autoimmune and inflammatory diseases.
Convergent evolution of the genomes of marine mammals OPEN   pp272 - 275
Andrew D Foote, Yue Liu, Gregg W C Thomas, Tomáš Vinař, Jessica Alföldi, Jixin Deng, Shannon Dugan, Cornelis E van Elk, Margaret E Hunter, Vandita Joshi, Ziad Khan, Christie Kovar, Sandra L Lee, Kerstin Lindblad-Toh, Annalaura Mancia, Rasmus Nielsen, Xiang Qin, Jiaxin Qu, Brian J Raney, Nagarjun Vijay, Jochen B W Wolf, Matthew W Hahn, Donna M Muzny, Kim C Worley, M Thomas P Gilbert & Richard A Gibbs
doi:10.1038/ng.3198
Andrew Foote and colleagues report the whole-genome sequences and de novo assemblies of three marine mammal species—the walrus, killer whale and manatee—and an improved bottlenose dolphin genome. Their comparative genomic analysis finds evidence of parallel evolution across the marine mammal genomes.

TECHNICAL REPORTS


A method for calculating probabilities of fitness consequences for point mutations across the human genome   pp276 - 283
Brad Gulko, Melissa J Hubisz, Ilan Gronau & Adam Siepel
doi:10.1038/ng.3196
Adam Siepel and colleagues develop a statistical method, fitCons, which combines comparative and functional genomic data to estimate the probability that a point mutation will influence fitness. They generate fitCons scores for three human cell types from ENCODE data sets and demonstrate improved prediction power for cis regulatory elements in comparison to conventional conservation-based scores.
Efficient Bayesian mixed-model analysis increases association power in large cohorts   pp284 - 290
Po-Ru Loh, George Tucker, Brendan K Bulik-Sullivan, Bjarni J Vilhjálmsson, Hilary K Finucane, Rany M Salem, Daniel I Chasman, Paul M Ridker, Benjamin M Neale, Bonnie Berger, Nick Patterson & Alkes L Price
doi:10.1038/ng.3190
Alkes Price, Po-Ru Loh and colleagues report the BOLT-LMM method for mixed-model association. They apply their method to 9 quantitative traits in 23,294 samples and demonstrate that it provides improvements in computational efficiency as well as gains in power that increase with the size of the cohort, making it useful for the analysis of large cohorts.
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies   pp291 - 295
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Nick Patterson, Mark J Daly, Alkes L Price & Benjamin M Neale
doi:10.1038/ng.3211
Benjamin Neale and colleagues report the LD Score regression method, used to distinguish the relative contributions of confounding bias and polygenicity to inflated test statistics in GWAS. They apply their method to summary statistics from GWAS for over 30 phenotypes, confirm that polygenicity accounts for the majority of inflation in test statistics and demonstrate use of this method as a correction factor.
Large multiallelic copy number variations in humans   pp296 - 303
Robert E Handsaker, Vanessa Van Doren, Jennifer R Berman, Giulio Genovese, Seva Kashin, Linda M Boettger & Steven A McCarroll
doi:10.1038/ng.3200
Steven McCarroll and colleagues report an analysis of multiallelic copy number variants (mCNVs). They characterize mCNVs in 849 whole-genome sequences from the 1000 Genomes Project and find that mCNVs give rise to most gene dosage variation in humans.

CORRIGENDA


Corrigendum: The genome sequence of the orchid Phalaenopsis equestris   p304
Jing Cai, Xin Liu, Kevin Vanneste, Sebastian Proost, Wen-Chieh Tsai, Ke-Wei Liu, Li-Jun Chen, Ying He, Qing Xu, Chao Bian, Zhijun Zheng, Fengming Sun, Weiqing Liu, Yu-Yun Hsiao, Zhao-Jun Pan, Chia-Chi Hsu, Ya-Ping Yang, Yi-Chin Hsu, Yu-Chen Chuang, Anne Dievart, Jean-Francois Dufayard, Xun Xu, Jun-Yi Wang, Jun Wang, Xin-Ju Xiao, Xue-Min Zhao, Rong Du, Guo-Qiang Zhang, Meina Wang, Yong-Yu Su, Gao-Chang Xie, Guo-Hui Liu, Li-Qiang Li, Lai-Qiang Huang, Yi-Bo Luo, Hong-Hwa Chen, Yves Van de Peer & Zhong-Jian Liu
doi:10.1038/ng0315-304a
Corrigendum: Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy   p304
Cas Simons, Lachlan D Rash, Joanna Crawford, Linlin Ma, Ben Cristofori-Armstrong, David Miller, Kelin Ru, Gregory J Baillie, Yasemin Alanay, Adeline Jacquinet, François-Guillaume Debray, Alain Verloes, Joseph Shen, Gözde Yesil, Serhat Guler, Adnan Yuksel, John G Cleary, Sean M Grimmond, Julie McGaughran, Glenn F King, Michael T Gabbett & Ryan J Taft
doi:10.1038/ng0315-304b

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